A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475121



Internal ID21132674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43558201..43562800hg38UCSC Ensembl
chr11:43579751..43584350hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991358
Samples
Known GenesMIR670
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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